Part 14: The Transition
My mother at ninety-four, July 2012, and as a young woman.
Saturday, March 9, 2013
Before I left for an afternoon appointment I was in touch with the aides and their supervisor. My mother was at home with three shifts of round the clock care and hospice nurses that were on twenty-four hour duty. My mother had more attention than she had ever dreamed of. But –there is always something for me to take care of and this time it was firing the day Hospice nurse. She had a cough. I complained. Loudly. They sent someone else.
My day was strange. I went to a close friend’s baby shower riddled with guilt that I was leaving the house. I told myself that I was allowed. The supervisor of the aides told me I had to go. In fact she insisted that I have a good time. I forgot what that means.
Once there I felt a little better but as soon as some of my former colleagues asked how I was, I couldn’t lie. I wanted to but was unable to. I wanted to say everything was perfect but I couldn’t. I sputtered, “My mother is dying.” Many of my friends lost their moms and I understood the words: their mothers had passed, they had no mothers. Now I can relate to the pain. People were nice, a few compassionate, but the fact is: most people don’t want to hear depressing stuff at a baby shower. I was assigned to camera duty and gratefully accepted. But as the afternoon progressed I got that sick feeling in my gut: I had to go home and face whatever was waiting for me.
Once back home I was hoping for a quiet evening but the internet was down and rebooting the router and modem didn’t fix the problem as it usually does. None of the computers or electronics would recognize the signal for a good period of time and then just as strangely as I got a tech from Verizon on the phone, all of a sudden things started working. Just as I was about to call I felt the fatigue I had been carrying on my back for months, six months, since my mother began to exhibit “signs.”
As the evening progressed my fatigue strengthened and I figured I’d go up to bed and give in to what I hoped would be sleep. All of a sudden there was a loud series of crashes and then broken glass.
Mind you, my cats never, NEVER have, in all the years I have them, jumped on a kitchen counter, EVER. But one must have, the one diagnosed with diabetes, smelled a cup of dry food on the counter and had likely leaped up and got stuck in something or spooked. He jumped through the pass through taking several crystal and glass pieces with him. It took me an hour to clean it all up and I am sure there are still some shards out there.
It felt like everything around me was different or in transition, that something bigger than myself was happening, I can’t explain it. Or maybe I can: things were falling apart. Or maybe the things around me were reflecting my feelings: I was in pieces.
And so to bed. You must understand that the fear of the phone ringing is one of my worst fears, that middle of the night call. It took me a long time to relax to drift into sleep.
This morning I had a long talk with the lovely replacement Hospice nurse. I learned that:
- my mother sat up in her chair for two hours yesterday and told her life story
- she sleeps most of the day
- she is barely drinking and there is barely any liquid output, a big difference from her having to go every couple of minutes
- she is refusing to take an anti-nausea medication, she said it makes her feel worse, except she didn’t take any, she only took her blood pressure meds
- she had sips of soup all day, and two small spoonfuls of mashed potato, today she had ice cream
- she is totally “with-it” and aware of everything
I was able to talk to her briefly and could barely comprehend her. She is just too tired, too weak to articulate. But what I did get was: I’m trying very hard to get well. My mother has always been a fighter, she’s tough, all, now, eighty-ish pounds of her. She is the last person alive in her family.
Today I wrote a stack of birthday and get well cards to send out tomorrow. Her ninety-fifth birthday is days away. These may be the last cards I ever send to my mother.
About four years ago I planned my mother’s funeral.
Today I went to the funeral home and paid the bill.
[This series is linked: see “continued here.” Also, below the line there will be links for the previous post and the next.]
I am so glad that you got your mom in a place of comfort for her. When my mom died it was sudden – a massive heart attack. But her heart was damaged from six months of chemo a few years prior. So when she went through her bout with breast cancer I had dealt mentally and emotionally with the prospect of losing her. That is the only justification I have ever come up with for the disease process – it gives us time to prepare for the inevitable eventual loss. I think the term in the business is called preparatory grieving. So what you are going through is normal. Although what you have accomplished for your mom as her advocate is extraordinary. Kuddos.
oops there is no edit button. The correct term is anticipatory grieving. Sorry.
And I see edit buttons, strange…
I have been through preparatory grieving several times. Yes, it does give us a chance to make peace but it is never easy. Thank you for the pat on the back as well, I needed that.
I am sorry you had to go through this with your mom. I guess it is all part of the human condition.
I wish I could be of comfort, my dear Sue. This is an awful period for everyone, me among the rest. This morning I was shocked to learn that one of my dearest friends, barely 61, had suddenly died yesterday. In any case I agree with Ann above: you need to look after yourself.
All my love, dearest.
Dani <3
I just saw your FB post, oh, so sorry! I’ve lost some friends well before their time, my best friend was 40 and lost in a strange accident. Sometimes I think it’s fate. So I’m with you and you’ve been with me and bottom line: we are all in this together. It’s very hard. Hugs and more …
She certainly looked great in July (and in all the photos throughout the years)! Love her hairdo, with that swoop detail on the right. Here’s hoping she feels well enough to keep that hair appointment she wanted you to make her, and celebrate her 95th in style!
Even though none of us will live forever, if she’s fighting to get better, my money is on her!
You need to look after Sue now.
In July I couldn’t keep up with her as she race through the mall: I was amazed. And then in September everything began to change–erratic blood pressure and vertigo started to diminish her. Still she remained independent and would call for ambulances and go into the hospital to get her pressure regulated. It never seemed to get stabilized.
The body just can do so much. She’s tired.
I am exhausted.
You have taken my breath away. Your advocacy for your mother is a standard that most of us can barely aspire to. Thank you for sharing her story and yours. Thank you for making us love your mother. And for worrying alongside you. I recently made my mother PROMISE to live forever because that’s how long I need her to be there for me — she laughed and promised — she thought I was kidding. But I’m not.
Dear Bonnie,
I was so happy to see you “here,” I thought this journey would have meaning for you. It’s harder for daughters and mothers I think. I am grateful that she lived this long, mainly medicine free (she studied homeopathy on her own and believed in natural remedies). But here she is, living alone, far away, independently until now, no friends left, many people in the assisted living have dementia, unable to relate.
It’s not easy if you live long–actually it is not easy if you just live. My big fear is that when my turn comes there won’t be anyone to advocate for me.
Grateful to see you.